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DIABETESMANAGER SYSTEM, DIABETESMANAGER-RX SYSTEM MODEL VERSION 1.1

K100066 Class II Traditional
Decision Date
2010-07-15
Sponsor / Applicant
Welldoc, Inc.

Technical Specification

510(k) Submission ID K100066
Product Code MRZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2010-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIABETESMANAGER SYSTEM, DIABETESMANAGER-RX SYSTEM MODEL VERSION 1.1 received FDA 510(k) clearance under submission number K100066, sponsored by Welldoc, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2010-07-15.

Classification & Regulation

This clearance is catalogued under FDA product code MRZ and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.